A synergistic antimicrobial composition containing flumetsulam and thiabendazole.
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1. A synergistic antimicrobial composition comprising:
(a) flumetsulam; and (b) thiabendazole; wherein a weight ratio of flumetsulam to thiabendazole is from 6:1 to 1:10.
3. The composition of
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This invention relates to combinations of biocides, the combinations having greater activity than would be observed for the individual antimicrobial compounds.
Use of combinations of at least two antimicrobial compounds can broaden potential markets, reduce use concentrations and costs, and reduce waste. In some cases, commercial antimicrobial compounds cannot provide effective control of microorganisms, even at high use concentrations, due to weak activity against certain types of microorganisms, e.g., those resistant to some antimicrobial compounds. Combinations of different antimicrobial compounds are sometimes used to provide overall control of microorganisms in a particular end use environment. For example, U.S. Pat. No. 5,591,760 discloses a combination of 3-iodo-2-propynyl-butylcarbamate (IPBC) and 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one (DCOIT), but this reference does not suggest any of the combinations claimed herein. Moreover, there is a need for additional combinations of antimicrobial compounds having enhanced activity against various strains of microorganisms to provide effective control of the microorganisms, especially in dry film coatings. The problem addressed by this invention is to provide such additional combinations of antimicrobial compounds.
The present invention is directed to a synergistic antimicrobial composition comprising: (a) flumetsulam; and (b) thiabendazole (TBZ); wherein a weight ratio of flumetsulam to thiabendazole is from 8:1 to 1:15.
As used herein, the following terms have the designated definitions, unless the context clearly indicates otherwise. Flumetsulam is N-(2,6-difluorophenyl)-5-methyl[1,2,4]triazolo[1,5-a]pyrimidine-2-sulfonamide. Diclosulam is N-(2,6-dichlorophenyl)-5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonamide. The term “antimicrobial compound” refers to a compound capable of inhibiting the growth of or controlling the growth of microorganisms; antimicrobial compounds include bactericides, bacteristats, fungicides, fungistats, algaecides and algistats, depending on the dose level applied, system conditions and the level of microbial control desired. The term “microorganism” includes, for example, fungi (such as yeast and mold), bacteria and algae. The following abbreviations are used throughout the specification: ppm=parts per million by weight (weight/weight), mL=milliliter, ATCC=American Type Culture Collection, and MIC=minimum inhibitory concentration. Unless otherwise specified, temperatures are in degrees centigrade (° C.), and references to percentages are by weight (wt %). Percentages of antimicrobial compounds in the composition of this invention are based on the total weight of active ingredients in the composition, i.e., the antimicrobial compounds themselves, exclusive of any amounts of solvents, carriers, dispersants, stabilizers or other materials which may be present.
Preferably, a weight ratio of flumetsulam to ZPT is from 8:1 to 1:12, preferably from 8:1 to 1:10, preferably from 7:1 to 1:12; preferably from 7:1 to 1:10; preferably from 6:1 to 1:12; preferably from 6:1 to 1:10; preferably from 6:1 to 1:8.
The antimicrobial compositions described above may contain other biocides. Typically, the antimicrobial compositions are used to inhibit growth of algae and/or fungi.
Preferably, the antimicrobial combinations of this invention are incorporated into liquid compositions, especially dispersions of polymers in aqueous media. The biocide combinations are particularly useful in preservation of building materials, e.g., adhesives, caulk, joint compound, sealant, wallboard, etc), paints, coatings, polymers, plastics, synthetic and natural rubber, paper products, fiberglass sheets, insulation, exterior insulating finishing systems, roofing and flooring felts, building plasters, wood products and wood-plastic composites. Preferably, the antimicrobial compositions are latex paints or other liquid coating compositions containing the biocide combinations disclosed herein. The biocide combinations are useful for preservation of the dry film coating resulting after application of a paint or other liquid coating composition. Preferably, the antimicrobial composition is an acrylic latex paint comprising one or more of the biocide combinations disclosed herein, or the dry film coating resulting from application of the paint to a surface.
Typically, the amount of the biocide combinations of the present invention to control the growth of microorganisms is from 100 ppm to 10,000 ppm active ingredient. Preferably, the active ingredients of the composition are present in an amount of at least 300 ppm, preferably at least 500 ppm, preferably at least 600 ppm, preferably at least 700 ppm. Preferably, the active ingredients of the composition are present in an amount of no more than 8,000 ppm, preferably no more than 6,000 ppm, preferably no more than 5,000 ppm, preferably no more than 4,000 ppm, preferably no more than 3,000 ppm, preferably no more than 2500 ppm, preferably no more than 2,000 ppm, preferably no more than 1,800 ppm, preferably no more than 1,600 ppm. Concentrations mentioned above are in a liquid composition containing the biocide combinations; biocide levels in the dry film coating will be higher.
The present invention also encompasses a method for preventing microbial growth in building materials, especially in dry film coatings, by incorporating any of the claimed biocide combinations into the materials.
Sample preparation: A single or blend of biocides was post added into white acrylic latex paint free of biocides to give a maximum total active ingredient/s concentration tested. This paint was then diluted with a biocide free acrylic latex paint to give targeted concentrations for the testing. Depending on the type of biocide blends tested, the total biocides concentrations varies from 200 to 5000 ppm. After biocides addition or dilution, each sample was hand mixed for at least a minute until uniformity is achieved. Each of the paint samples as well as a control sample (containing no biocide) were used to prepare films on black plastic-vinyl chloride/acetate copolymer panels (LENETA, Mahwah, N.J.) using a 3 mil (0.0762 mm) bird bar applicator. The panels were thoroughly dried for at least 2 days avoiding direct exposure to sunlight. Square discs (0.5 inch; 1.27 cm2) were cut out from each panel and were used as the substrate for fungal and algal efficacy tests. This sample size allowed for an agar border when the sample disc was placed into the well of the test plate. Each sample was tested in duplicate
Test Conditions:
The appropriate media (BOLD'S 3N for Chlorophytes, BG-11 for Cyanobacteria, and PDA for fungi) were used to support microbial growth. The test plates were maintained at room temp (25° C.-26° C.), in a cycled light-dark environment, for four weeks for algae. Plates for fungal challenge tests were maintained at 30 C for four weeks. At the end of the incubation period the samples were scored for percent area covered by visible microbial growth.
Algal Inoculum
Medium for
Organisms
abbreviation
Type
testing
Gloeocapsa sp.
Gs
ATCC 29159
Unicellular,
BG-11
Colonial
Cyanobacteria
Oscillatoria sp.
Os
ATCC 29135
Filamentous
BG-11
Cyanobacteria
Nostoc commune
Nc
CCAP 1453/29
Unicellular,
Bold
Cenobial
Chlorophyte
Trentepohlia aurea +
Ta + To
UTEX LB 429 +
Filamentous
Bold
Trentepohlia odorata
CCAP 483/4
Chlorophyte
Chlorella sp. UTEX +
Cs + Ck
ATCC 30582 +
Unicellular
Bold
Chlorella kessleri
ATCC 11468
Chlorophyte
Calothrix parientina
Cp
UTEX LB 1952
Filamentous
Bold
Cyanobacteria
Fungal Inoculum
Medium for
Organisms
abbreviation
ATCC#
Growth and Testing
Aspergillus niger
An
9642
PDA
Penicillium funiculosum
Pf
11797
PDA
Cladosporium herbarum
Ch
11281
PDA
Aureobasidium pullulans
Ap
9348
PDA
Trichoderma viride
Tv
32630
PDA
Alternaria alternata
Aa
20084
PDA
Algal Efficacy Testing
Modified ASTM 5589
ASTM 5589 is a standard accelerated test method for determining resistance of various coatings (including paints) to algal defacement. To accommodate for high-throughput screening, this method was scaled down from petri plates to 6-well plates. A single coupon was placed with a pair of sterile forceps at the center of the agar plug (on top) with the painted surface facing upwards. Algal inoculums were prepared by mixing equal concentrations (1×106 cfu/ml) and equal volumes (depending on number of samples to be inoculated) of like growing organisms.
In Flumetsulam+various IT synergy study, three pool of mixed algae were prepared as the test inoculum, Gloeocapsa sp. and Oscillatoria sp. a mix of cyanobacteria grown on BG-11 media; Chlorella sp., Chlorella kessleri, and Nostoc commune are unicellular chlorphytes that were mixed and grown on Bold media; Trentepohlia aurea, Tretepohlia odorata, and Calotrix parientina are filamentous algae that were mixed and grown on Bold media.
In Diclosulam+various IT synergy study, only two pools of mixed algae were prepared; Gloeocapsa sp. and Oscillatoria sp. grown on BG-11 media and Chlorella sp., Chlorella kessleri, Nostoc commune, Trentepohlia aurea, Tretepohlia odorata, and Calotrix parientina grown on Bold media
Each well that contains a tested coupon was inoculated with 400 μl of organism mixture (1×106 cfu/ml) making sure that the whole surface (paint film as well as the agar surrounding it) was evenly covered. The plates were incubated at room temp (25° C.-26° C.) with cyclic exposure to light (OTT-Lite model # OTL4012P, 40 Watt, 26 KLumen) and dark phases, for a period of four weeks. The total area covered was evaluated at the end of each week according to percent area covered in 5% increments.
Fungal Efficacy Testing—Modified ASTM 5590
ASTM 5590 is a standard accelerated test method for determining resistance of various coatings (including paints) to fungal defacement. To accommodate for high-throughput screening, this method was scaled down from petri plates to 6-well plates. To set up the test, an agar plug was placed at the bottom of each well of the sterile 6-well plate. A single coupon was placed with a pair of sterile forceps at the center of the agar plug (on top) with the painted surface facing upwards. Fungal inoculums were prepared by mixing equal concentrations (1×106 cfu/ml) and equal volumes (depending on number of samples to be tested) of like growing organisms. For Flumetsulam+various IT synergy study, three pools of mixed fungi were prepared as the test inoculum. Cladosporium herbarum was mixed with Aureobasidium pullulans; Aspergillus niger was mixed with Penicillium funiculosum and Alternaria alternata was mixed with Trichoderma viride. For Diclosulam+various IT synergy study, all above fungi were mixed as a single pool. Each well was inoculated with 400 μl of organism mixture (1×106 cfu/ml) making sure that the whole surface (paint film as well as the agar surrounding it) was evenly covered. The plates were incubated at 30° C. in presence of moisture, for a period of four weeks. The total percent area covered was evaluated and recorded at the end of each week after the 2nd week and recorded in increments of 5%.
Synergy Index Calculation
Synergy Index (SI)
The SI is calculated based on F. C. Kull et. Al. method (Applied Microbiology, Vol. 9 (1961). In this study, SI was calculated based on the following formula with the minimum inhibitory concentration chosen based on the percent inhibitory exhibited by the individual biocide against each microorganisms tested.
SI=Qa/QA+Qb/QB
Flumetsulam: TBZ Synergy study
Cp +
Cs +
AaTv
AnPf
ApCh
To + Ta
Ck + Nc
Gs + Os
1Flumet:
1TBZ
Total conc,
1000
1000
1000
4000
4000
2000
ppm
% inhibition
100
100
100
40
100
90
SI
<0.94
1.1
0.9
1.7
1.6
0.7
1Flumet:
3TBZ
Total conc,
1000
1000
1000
4000
3000
2000
ppm
% inhibition
100.0
100
100
90
100
90
SI
<1.27
1.3
1.3
1.4
1.2
0.6
1Flumet:
5TBZ
Total conc,
900
900
900
3600
3600
900
ppm
% inhibition
100
100
100
50
50
100
SI
<1.24
1.3
1.2
1.1
1.4
0.3
1Flumet:
10TBZ
Total conc,
962.5
962.5
962.5
3850
3850
2888
ppm
% inhibition
100
90
100
40
40
90
SI
<1.43
1.5
1.4
1.1
1.5
0.8
6Flumet:
1TBZ
Total conc,
875
875
1750
3500
3500
875
ppm
% inhibition
100
100
100
40
40
90
SI
<0.41
0.7
0.8
1.9
1.3
0.3
4Flumet:
1TBZ
Total conc,
937.5
937.5
937.5
2813
3750
1875
ppm
% inhibition
100
90
100
80
70
90
SI
<0.51
0.7
0.5
1.4
1.4
0.7
2Flumet:
1TBZ
Total conc,
937.5
37.5
3750
2813
3750
2813
ppm
% inhibition
100
95
100
90
70
100
SI
<0.68
0.9
2.7
1.3
1.5
1.0
Flumetsulam
Total conc,
3500
1750
3500
1750
2625
2625
ppm
% inhibition
0
90
50
75
100
90
TBZ
Total conc,
625
625
625
3750
2500
3750
ppm
% inhibition
100
100
100
90
100
85
Note:
If any of the active with maximum concentration tested did not exhibit some inhibition, this maximum concentration is used to calculate the estimated SI and a sign of less than (<) is included to take into account that higher concentration of the active is needed to achieve the targeted inhibition
NE = no end point at the concentration tested that will meet the percent inhibition criteria set in each SI calculation
Synergy study of Diclosulam and TBZ
Aa + Tv + An +
Cp + To + Ta +
Ratios
Pf + Ap + Ch
Cs + Ck + Nc
Gs + Os
1Diclosulam: 1 TBZ
Total conc, ppm
1500
3000
3000
% inhibition
60
100
100
SI
1.4
2.1
2.9
3Dicolosulam: 1 TBZ
Total conc, ppm
2250
3000
750
% inhibition
60
50
90
SI
1.4
1.9
1.8
5Diclosulam: 1 TBZ
Total conc, ppm
300
3000
3000
% inhibition
50
80
100
SI
1.5
1.8
4.1
10Diclosulam: 1 TBZ
Total conc, ppm
2750
2750
687.5
% inhibition
50
80
95
SI
1.1
1.6
1.9
1Diclosulam: 10 TBZ
Total conc, ppm
3000
3300
825
% inhibition
50
80
90
SI
4.9
2.6
1.3
1Diclosulam: 6 TBZ
Total conc, ppm
2800
2800
2800
% inhibition
50
95
100
SI
4.0
2.1
1.7
1Diclosulam: 4 TBZ
Total conc, ppm
3250
3250
812.5
% inhibition
50
90
100
SI
4.3
2.5
1.4
1Diclosulam: 2 TBZ
Total conc, ppm
3000
3000
750
% inhibition
60
75
100
SI
3.5
2.2
1.5
Diclosulam
Total conc, ppm
3500
1750
875
% inhibition
0
100
90
TBZ
Total conc, ppm
625
1250
1250
% inhibition
60
100
85
Patent | Priority | Assignee | Title |
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